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http://purl.uniprot.org/citations/23125284http://purl.uniprot.org/core/author"Szklarczyk R."xsd:string
http://purl.uniprot.org/uniprot/#_B3KM21-mappedCitation-23125284http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23125284
http://purl.uniprot.org/uniprot/Q5RI15http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/23125284
http://purl.uniprot.org/citations/23125284http://purl.uniprot.org/core/date"2013"xsd:gYear
http://purl.uniprot.org/uniprot/P00403http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/23125284
http://purl.uniprot.org/citations/23125284http://purl.uniprot.org/core/author"Veltman J.A."xsd:string
http://purl.uniprot.org/citations/23125284http://purl.uniprot.org/core/author"Koopman W.J."xsd:string
http://purl.uniprot.org/uniprot/P00403#attribution-9CA48482B293BFF4C97EA66198B3EB33http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/23125284
http://purl.uniprot.org/uniprot/Q5RI15#attribution-30BD78EB6232AD309817CD7511000603http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/23125284
http://purl.uniprot.org/citations/23125284http://purl.uniprot.org/core/author"van den Brand M.A."xsd:string
http://purl.uniprot.org/citations/23125284http://purl.uniprot.org/core/volume"22"xsd:string
http://purl.uniprot.org/citations/23125284http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/23125284http://purl.uniprot.org/core/name"Hum. Mol. Genet."xsd:string
http://purl.uniprot.org/citations/23125284http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/23125284
http://purl.uniprot.org/citations/23125284http://purl.uniprot.org/core/author"Willems P.H."xsd:string
http://purl.uniprot.org/citations/23125284http://purl.uniprot.org/core/author"Nooteboom M."xsd:string
http://purl.uniprot.org/citations/23125284http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/23125284
http://purl.uniprot.org/uniprot/#_Q5RI15-citation-23125284http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23125284
http://purl.uniprot.org/citations/23125284http://purl.uniprot.org/core/author"Hendriks-Franssen M.G."xsd:string
http://purl.uniprot.org/uniprot/Q5RI15#attribution-48C8F70EE1D927F010B3D88C86DD706Dhttp://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/23125284
http://purl.uniprot.org/uniprot/Q5RI15#attribution-C317B9D4C503DF1442B3537880764176http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/23125284
http://purl.uniprot.org/citations/23125284http://purl.uniprot.org/core/title"A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia."xsd:string
http://purl.uniprot.org/uniprot/#_P00403-citation-23125284http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23125284
http://purl.uniprot.org/citations/23125284http://purl.uniprot.org/core/pages"656-667"xsd:string
http://purl.uniprot.org/citations/23125284http://purl.uniprot.org/core/author"Dikow N."xsd:string